Venous Insufficiency Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A vein disease that is characterized by impaired flow of blood through the veins. (Human Disease Ontology, DOID_10128)
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Genes

6 genes associated with the Venous Insufficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
COL1A2 collagen, type I, alpha 2
CYP2A6 cytochrome P450, family 2, subfamily A, polypeptide 6
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1